JPS63132947A - Method for treating molded polyamide article - Google Patents
Method for treating molded polyamide articleInfo
- Publication number
- JPS63132947A JPS63132947A JP27922086A JP27922086A JPS63132947A JP S63132947 A JPS63132947 A JP S63132947A JP 27922086 A JP27922086 A JP 27922086A JP 27922086 A JP27922086 A JP 27922086A JP S63132947 A JPS63132947 A JP S63132947A
- Authority
- JP
- Japan
- Prior art keywords
- lubricating oil
- polyamide
- lubricant
- water
- molded
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000004952 Polyamide Substances 0.000 title claims abstract description 27
- 229920002647 polyamide Polymers 0.000 title claims abstract description 27
- 238000000034 method Methods 0.000 title claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000010687 lubricating oil Substances 0.000 claims abstract description 24
- 239000000839 emulsion Substances 0.000 claims abstract description 12
- 238000000465 moulding Methods 0.000 claims abstract description 8
- 238000010438 heat treatment Methods 0.000 claims abstract description 5
- 238000001035 drying Methods 0.000 claims abstract description 4
- 239000000314 lubricant Substances 0.000 abstract description 14
- 238000010521 absorption reaction Methods 0.000 abstract description 13
- 229920002545 silicone oil Polymers 0.000 abstract description 9
- 238000011282 treatment Methods 0.000 abstract description 9
- 238000005299 abrasion Methods 0.000 abstract description 5
- 230000006866 deterioration Effects 0.000 abstract description 5
- 239000003995 emulsifying agent Substances 0.000 abstract description 3
- 239000007788 liquid Substances 0.000 abstract description 3
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 2
- 239000011248 coating agent Substances 0.000 abstract description 2
- 238000000576 coating method Methods 0.000 abstract description 2
- 229930195733 hydrocarbon Natural products 0.000 abstract description 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 239000003208 petroleum Substances 0.000 abstract description 2
- 238000007598 dipping method Methods 0.000 abstract 1
- 239000004519 grease Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 239000004677 Nylon Substances 0.000 description 6
- 229920001778 nylon Polymers 0.000 description 6
- 239000010410 layer Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 208000005156 Dehydration Diseases 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 238000005461 lubrication Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000003754 machining Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000012805 post-processing Methods 0.000 description 2
- 238000002203 pretreatment Methods 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000009750 centrifugal casting Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明はポリアミド成形品の処理方法に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] This invention relates to a method for treating polyamide molded articles.
ポリアミドとは、通常酸アミド結合(−C0N)I −
→を有する重合体の総称であって、そのうち繊維形成能
のある線状食合体をナイロンと呼び、たとえばナイロン
6、ナイロン46、ナイロン66、ナイロン610、ナ
イロン7、ナイロン8、ナイロン9、ナイロン10.ナ
イロン11.ナイロン12などまたはこれらの共重合も
しくは混合したものなど数多くのものが工業的規模で生
産されていることはすでによく知られている。そして、
このようなポリアミドはほかのプラスチックおよび金属
材料と比較すると、機械的強さ、特に耐摩耗性、自己潤
滑性、軽量性、成形性、耐熱耐寒性、無音性、耐薬品性
、無毒性、染色性などの多くの点ですぐれていて、プラ
スチック材料の分野では、軸受、ブツシュ、歯車、自動
車その他車両用部品等の各種機器部品に広く活用されて
いる。また繊維材料の分野で絹に代わる合成繊維として
重要視されていることもよく知られている。しかし、こ
のポリアミドは主鎖にあるカルボニル基(=C−0)の
酸素とその隣接アミノ基(=N11)の水素との間に分
子力(水素結合)が作用し、このような群が親水性であ
るために、湿潤空気中に放置すると湿気を吸着したり、
または乾燥空気中に放置すると吸収水分を放出して、吸
収率がθ〜14%程度の範囲で変動して、そのポリマー
の種類によって程度の差はあるが、そのときの吸収量に
よってその成形品の機械的諸性質は大きく影響を受ける
ので、比較的多量の水分を吸収した状態で耐摩耗性、潤
滑性、耐衝撃性などの機械的諸性質がたとえすぐれた成
形品であったとしても、吸水量の減少に伴い性能が低下
して使用に耐えなくなり、各種トラブルの原因となるこ
ともしばしばある。したがって、ポリアミドのこのよう
な吸水性は一つの致命的な欠陥であり、従来から耐摩耗
性、潤滑性等を強化するために、水潤滑、固体潤滑剤(
たとえば二硫化モリブデン、黒鉛、金属石けん等)添加
、油潤滑等の方法が採用されて来たが、吸水量を本質的
に調整し安定化し、耐摩耗性、潤滑性、耐衝撃性を向上
させようとする試みはほとんど見られなかった。Polyamide is usually an acid amide bond (-C0N) I-
→ It is a general term for polymers having a fiber-forming ability, and among them, linear fiber-forming polymers are called nylon, such as nylon 6, nylon 46, nylon 66, nylon 610, nylon 7, nylon 8, nylon 9, nylon 10. .. Nylon 11. It is already well known that a large number of materials such as nylon 12 or their copolymers or mixtures are produced on an industrial scale. and,
Compared to other plastic and metal materials, such polyamides have excellent mechanical strength, especially abrasion resistance, self-lubricating properties, light weight, moldability, heat and cold resistance, silence, chemical resistance, non-toxicity, and dye resistance. It is excellent in many respects, such as its properties, and in the field of plastic materials, it is widely used in various equipment parts such as bearings, bushes, gears, automobiles and other vehicle parts. It is also well known that in the field of textile materials, it is considered important as a synthetic fiber that can replace silk. However, in this polyamide, molecular force (hydrogen bond) acts between the oxygen of the carbonyl group (=C-0) in the main chain and the hydrogen of the adjacent amino group (=N11), and these groups become hydrophilic. Due to its nature, it may absorb moisture if left in humid air.
Or, if left in dry air, the absorbed moisture will be released, and the absorption rate will fluctuate in the range of θ to 14%.The degree of absorption varies depending on the type of polymer, but the amount of absorption at that time will affect the molded product. The mechanical properties of molded products are greatly affected, so even if a molded product has excellent mechanical properties such as abrasion resistance, lubricity, and impact resistance after absorbing a relatively large amount of water, As the amount of water absorbed decreases, the performance deteriorates, making it unusable and often causing various troubles. Therefore, this kind of water absorption of polyamide is a fatal flaw, and conventionally, water lubrication, solid lubricant (
For example, methods such as adding molybdenum disulfide, graphite, metal soap, etc.) and oil lubrication have been adopted, but methods such as essentially adjusting and stabilizing water absorption and improving wear resistance, lubricity, and impact resistance have been adopted. There were almost no attempts to do so.
そこでこの発明の発明者は特願昭58−69818号に
よって表面に水および潤滑油の浸透層を設けたことを特
徴とするポリアミド製機械部品および成形後吸水処理お
よび脱水処理を行ない、さらに水系エマルジョン型潤滑
油を加熱浸透させることを特徴とするポリアミド製機械
部品の製造方法を開示した。このようにポリアミド成形
品の表面に水および潤滑油の浸透層が設けられるとポリ
アミド本来の潤滑性を著しく向上させると同時に、ポリ
アミドの欠点である吸水量の変動に基づく耐衝撃性、耐
摩耗性等の機械的性能の劣化防止に対しても顕著な効果
を示し、後加工後の寸法安定性も著しく改善したのであ
る。しかし、このようなポリアミド成形品を製造するた
めに開示した方法は、通常70℃程度以上の熱湯もしく
は120℃程度以下の水蒸気の雰囲気中に数時間ないし
数十時間浸漬もしくは封入してポリアミド成形品に強制
的に水分を吸収させた後、たとえば70〜120℃程度
に加熱しそのうえたとえば数十@1−11gもしくはそ
れ以下に減圧して吸収させた水分を脱離させて、その後
成形品に水系エマルジョン型潤滑油を加熱浸透させると
いうものであるが、前処理である成形後の吸水処理およ
び脱水処理はきわめて繁雑であるという欠点がある。Therefore, the inventor of the present invention proposed a polyamide machine part characterized by having a water and lubricant permeation layer on its surface, water absorption treatment and dehydration treatment after molding, and further developed a water-based emulsion in accordance with Japanese Patent Application No. 58-69818. A method for manufacturing polyamide mechanical parts is disclosed, which is characterized by heating and infiltrating mold lubricating oil. When a water and lubricating oil permeation layer is provided on the surface of a polyamide molded product in this way, it significantly improves the inherent lubricity of polyamide, and at the same time improves impact resistance and abrasion resistance due to fluctuations in water absorption, which are disadvantages of polyamide. It also showed a remarkable effect in preventing deterioration of mechanical performance such as, etc., and the dimensional stability after post-processing was also significantly improved. However, the method disclosed for producing such polyamide molded products usually involves immersing or enclosing the polyamide molded product in an atmosphere of hot water of about 70°C or higher or steam of about 120°C or lower for several hours to several tens of hours. After forcibly absorbing water, the water is heated to, for example, about 70 to 120°C, and then the pressure is reduced to, for example, several tens of 1 to 11 g or less to remove the absorbed water. Although the emulsion-type lubricating oil is heated and permeated, the disadvantage is that the pre-treatments, such as water absorption treatment and dehydration treatment after molding, are extremely complicated.
このように従来の技術においては諸性質の著しく改善さ
れたポリアミド成形品が得られても、それを得るための
処理方法が繁雑であるという問題点があった。As described above, although a polyamide molded article with significantly improved properties can be obtained in the conventional techniques, there is a problem in that the processing method for obtaining it is complicated.
上記の問題点を解決するために、この発明は成形後に水
系エマルジョン型潤滑油を浸透させ、常温下もしくは加
熱下で潤滑油を充分定着させさらに乾燥させてポリアミ
ド成形品を処理するという手段を採用したものである。In order to solve the above problems, this invention adopts a method of treating polyamide molded products by infiltrating a water-based emulsion type lubricating oil after molding, fixing the lubricating oil sufficiently at room temperature or under heating, and then drying it. This is what I did.
以下その詳細を述べる。The details will be described below.
まず、この発明における水系エマルジタン型潤滑油とは
常温で液状もしくは半固体状(グリース状)の潤滑剤(
たとえば高分子量炭化水素成分を主体とする石油系のも
のまたはオレフィン重合油、ジエステル油、ポリアルキ
レングリコール油、ハロゲン化炭化水素油、シリコーン
油のような合成油、動植物油等の単独もしくはこれらの
二種以上の混合油またはこれら油類に酸アミド基に対し
て反応性のある基たとえば水酸基、カルボキシル基、エ
ポキシ基などを導入し変性したもの、さらには潤滑剤と
して要求される改質剤を添加したものなど)を乳化剤を
添加して水に分散させたものであり、乳化剤を親水性の
たとえば石けんもしくはアルコール類のような水溶性の
ものとすれば潤滑油を透明な状態で水に溶解させること
も可能である。First, the water-based emulgitane lubricant in this invention is a lubricant that is liquid or semi-solid (grease-like) at room temperature.
For example, petroleum-based oils mainly containing high molecular weight hydrocarbon components, synthetic oils such as olefin polymerized oils, diester oils, polyalkylene glycol oils, halogenated hydrocarbon oils, silicone oils, animal and vegetable oils, etc. alone or in combination. Mixed oils of more than one species, or modified oils by introducing groups reactive to acid amide groups, such as hydroxyl groups, carboxyl groups, epoxy groups, etc., and addition of modifiers required as lubricants. lubricating oil is dispersed in water by adding an emulsifier.If the emulsifier is hydrophilic and water-soluble, such as soap or alcohol, the lubricating oil will be dissolved in water in a transparent state. It is also possible.
ここで、潤滑油の種類によっては触媒作用を有する第三
物質を添加し、浸透層内で重合反応を起こさせて分子量
のより大きい潤滑剤に変化させることもできる。さらに
潤滑油エマルジョンを適宜着色しておけば成形品表面の
着色が可能であり色彩的効果が得られると同時に、成形
品表面の浸透層の厚さを知るうえで好都合である。Here, depending on the type of lubricant, a third substance having a catalytic effect may be added to cause a polymerization reaction within the permeation layer to change the lubricant to a lubricant with a larger molecular weight. Furthermore, if the lubricating oil emulsion is appropriately colored, it is possible to color the surface of the molded product and obtain a color effect, and at the same time, it is convenient for knowing the thickness of the permeation layer on the surface of the molded product.
つぎに、この発明におけるポリアミドは特に種類を限定
するものではなく、カーボンブラックその他の顔料、充
填材または強化材等を適宜含有するものでもよく、従来
からエンジニアリングプラスチックまたは繊維材料等の
分野で広く用いられているものであればいずれであって
もよい。通常ポリアミドは約200〜320℃程度の温
度のもとに行なわれる射出成形、押出成形、紡糸などの
ほか吹込成形、フィルム(シート)成形、焼結成形、遠
心鋳造、粉末被覆法、モノマーキャスティング、機械加
工等によって各種各様の成形品が得られる。Next, the type of polyamide used in the present invention is not particularly limited, and may contain carbon black, other pigments, fillers, reinforcing materials, etc., and has been widely used in the fields of engineering plastics and fiber materials. Any of the following may be used. Polyamides are usually processed by injection molding, extrusion molding, spinning, etc., which are carried out at temperatures of approximately 200 to 320°C, as well as blow molding, film (sheet) molding, sinter molding, centrifugal casting, powder coating, monomer casting, etc. Various molded products can be obtained by machining etc.
また、ポリアミド成形品は成形後の経過時間が短く、接
触する雰囲気が乾燥しているほど成形品の吸水量が少な
くて好ましい、このような成形品に水系エマルジョン型
潤滑油を浸透させるにあたっては、特に温度または時間
などを限定するものではないが、一般に温度が低い程処
理時間を長(する必要があり、また処理時間を短くする
うえで高い温度が望ましいからといって、高温にする程
設備費、経費等が増加して経済的不利を招くので、通常
の場合70〜120℃程度の温度のもとで成形品に水系
エマルジョン型潤滑油を塗布するかまたは成形品を水系
エマルジョン型潤滑油中に浸漬して、数十時間もしくは
それ以内の間、成形品の表面が潤滑油エマルジョンで充
分に覆われた状態に保っておけばよい、つぎに、このよ
うな処理を終わった成形品に対して、好ましくは付着し
ている過剰の潤滑油エマルジョンを除去した後、常温下
または加熱下で浸透した潤滑油の定着処理が施される。In addition, polyamide molded products have a short elapsed time after molding, and the drier the contact atmosphere, the less water absorption of the molded product, which is preferable.In infiltrating water-based emulsion type lubricating oil into such molded products, Although there are no particular limitations on temperature or time, in general, the lower the temperature, the longer the processing time (necessary), and even though a higher temperature is desirable to shorten the processing time, the higher the temperature, the more equipment Since this will increase costs and costs, resulting in an economic disadvantage, normally a water-based emulsion type lubricant is applied to the molded product at a temperature of about 70 to 120°C, or a water-based emulsion type lubricant is applied to the molded product at a temperature of about 70 to 120°C. The surface of the molded product can be kept fully covered with the lubricating oil emulsion for several tens of hours or less. On the other hand, after removing the excess lubricating oil emulsion that has adhered, preferably, the infiltrated lubricating oil is fixed at room temperature or under heating.
この定着処理中の潤滑油の挙動については詳らかでない
節もあるが、潤滑油自身の結合または潤滑油の分子に自
然にもしくは人工的に導入された反応基とポリアミドと
の結合等によって成形品の潤滑油が浸透した部分に新た
に強固な組織が形成されるものと推定される。そしてこ
のような定着処理中の各種反応は通常高温(ただし成形
品の軟化点よりも低温)であるほど速度が大きく有利で
あるが、成形品が著しく偏肉していたり、複雑な形状の
ものであったり、潤滑油が熱変質しやすいものであるよ
うなときには常温下で行なわれることが望ましい。The behavior of the lubricating oil during this fixing process is not entirely clear, but the molded product is formed by the bonding of the lubricating oil itself or the bonding of reactive groups naturally or artificially introduced into the lubricating oil molecule with the polyamide. It is presumed that a new strong structure is formed in the area where the lubricating oil has penetrated. Generally, the higher the temperature (lower than the softening point of the molded product), the faster the various reactions during the fixing process, which is advantageous. In cases where the lubricating oil is susceptible to thermal deterioration, it is desirable to carry out the process at room temperature.
さらに、このような定着処理の後には、乾燥処理が行な
われるが、これは潤滑油の定着をより完全なものにする
と同時に過剰の水分を脱離させるための処理であり、定
着処理の延長としてまたは切り離して別条性下で実施さ
れてもよく、その具体的方法は乾燥空気、温風、熱風等
を利用する通常の方法でよく、成形品の重量変化のなく
なる時点をもって終点とすればよい。Furthermore, after such a fixing process, a drying process is performed, which is a process to make the fixing of the lubricant more complete and at the same time remove excess moisture, and as an extension of the fixing process. Alternatively, it may be carried out separately in separate strips, and the specific method may be a normal method using dry air, warm air, hot air, etc., and the end point may be the point at which the weight of the molded product stops changing. .
なお、軸受、ブツシュ、歯車その他の高晴度が要求され
る成形品については、最後に改めて仕上げのための機械
加工を施してもよい。In addition, for bearings, bushings, gears, and other molded products that require high clearness, machining may be performed again for finishing at the end.
以下に実施例および比較例を示す。 Examples and comparative examples are shown below.
実施例:
ポリアミド〔東し社製:ナイロンCM10171をシリ
ンダ一温度270〜280℃で成形金型内に射出し、金
型内で80℃まで冷却した後取り出して、外径1911
内径7■畷、幅9箇−の車の両側面に、深さ約2鶴で扇
形状の三つのくぼみが3カ所に約2.5Mの間隔をおい
て同心円状に配列している摺動用の車輪を得た。この車
輪を80℃のシリコーン油溶解水液(シリコーン油(東
し社製:シリコーンTK20“〕を約40%含有し親水
性界面活性剤によって均一分散させ、浸透層の厚さを検
知しやすくするために少量の着色剤を加えて茶褐色液と
したもの)に投入し、同温度に保持しながら約48時間
浸漬し、車輪表面層に水およびシリコーン油を充分に吸
収させ、約0.1u厚の浸透層を形成させた。その後こ
れを約120℃に加熱して、浸透した潤滑油の定着処理
および引き続いて乾燥処理を行なった。所要時間は約1
0時間であった。得られた車輪の機械的性質を評価する
ために、シリコーン油溶解水液処理を施さない射出成形
後そのままの同形状の車輪を対照品として、3000k
trのr@重回転試験を試みた結果、この発明による実
施例で得た車輪は8力月経過後においてもなお荷重に耐
えていたのに対して、対照品は800kgの荷重回転試
験でわずかに2〜3時間のうちに摩滅破壊し使用するこ
とが出来なくなった。そして、この発明による車輪は大
気中の湿度に影響されることなく、前記特願昭58−6
9818号で開示した吸水処理および脱水処理を前処理
として行なう方法に勝るとも劣らない緒特性を兼ね備え
たものであった1以上の傾向はたとえば綿実油のような
シリコーン油以外の潤滑油で処理したときも同様であっ
た。Example: Polyamide [manufactured by Toshi Co., Ltd.: Nylon CM10171] was injected into a mold at a cylinder temperature of 270 to 280°C, cooled to 80°C in the mold, taken out, and made into an outer diameter of 1911°C.
On both sides of the car, which has an inner diameter of 7 inches and a width of 9 holes, there are three fan-shaped depressions about 2 cranes deep and arranged concentrically at three locations at intervals of about 2.5 m.For sliding purposes. got wheels. This wheel is uniformly dispersed in an 80°C silicone oil solution (containing approximately 40% silicone oil (manufactured by Toshisha Co., Ltd.: Silicone TK20)) using a hydrophilic surfactant to make it easier to detect the thickness of the permeation layer. A small amount of coloring agent was added to make a brownish liquid), and the wheel was soaked for about 48 hours while being maintained at the same temperature to fully absorb water and silicone oil into the wheel surface layer. This was then heated to about 120° C. to fix the penetrating lubricating oil, and then dry it. The time required was about 1.
It was 0 hours. In order to evaluate the mechanical properties of the obtained wheel, a wheel of the same shape after injection molding without silicone oil solution treatment was used as a control product.
As a result of trying the r @ heavy rotation test of tr, it was found that the wheel obtained in the example according to the present invention still withstood the load even after 8 months had passed, whereas the control product could only withstand the load in the 800 kg load rotation test. It wore out and broke within 2 to 3 hours and became unusable. The wheels according to the present invention are not affected by the humidity in the atmosphere.
One or more of the characteristics that were comparable to the method disclosed in No. 9818 in which water absorption treatment and dehydration treatment are performed as pre-treatments were obtained when treated with a lubricating oil other than silicone oil, such as cottonseed oil. The same was true.
比較例:
上記実施例と同じ条件で射出成形して得た車輪を80℃
に加熱したシリコーン油(実施例と同一品で水分を含ま
ない)に約48時間浸潤した。得られた車輪の3000
hg荷重回転試験の結果は実施例の車輪と大差はなく、
シリコーン油の付着が潤滑作用に影響したものと考えら
れるが、5 kgの落錘片を2mの高さから落下させる
落錘衝撃試験では、実施例で得た定着処理および乾燥処
理済みの車輪に異状は認められなかったが、この比較例
で得た車輪は破壊し、耐衝撃性の著しく劣ることが明ら
かとなった。Comparative example: A wheel obtained by injection molding under the same conditions as the above example was heated to 80°C.
The sample was soaked in silicone oil (the same product as in the example, but did not contain water) heated to about 48 hours. 3000 of the wheels obtained
The results of the hg load rotation test were not much different from the wheels of the example.
It is thought that the adhesion of silicone oil affected the lubrication effect, but in a falling weight impact test in which a 5 kg falling weight piece was dropped from a height of 2 m, it was found that the fixed and dried wheels obtained in the example Although no abnormality was observed, the wheel obtained in this comparative example was destroyed, and it became clear that the impact resistance was significantly inferior.
以上の処理を施されたこの発明のポリアミド成形品は、
成形品の組織内に形成された水および潤滑油の浸i3N
の作用機構によって、ポリアミド本来の潤滑性を著しく
向上させると同時に、ポリアミドの欠点である吸水量の
変動暢基づく耐衝撃性、耐摩耗性、引張り強度等の機械
てく特性の劣化の防止に対しても顕著な効果を示し、ま
た、後加工後の寸法安定性もきわめてすぐれている。こ
のような好結果が簡単な処理によって得られるのである
から、この発明の意義はきわめて大きいと言える。The polyamide molded product of this invention subjected to the above treatment is
Immersion of water and lubricating oil formed within the structure of the molded product i3N
This mechanism of action significantly improves the inherent lubricity of polyamide, and at the same time prevents the deterioration of mechanical properties such as impact resistance, abrasion resistance, and tensile strength due to fluctuations in water absorption, which are disadvantages of polyamide. Also, the dimensional stability after post-processing is extremely good. Since such good results can be obtained through simple processing, it can be said that the significance of this invention is extremely large.
Claims (1)
しくは加熱下で潤滑油を充分定着させさらに乾燥するこ
とを特徴とするポリアミド成形品の処理方法。A method for treating a polyamide molded article, which comprises infiltrating a water-based emulsion type lubricating oil after molding, sufficiently fixing the lubricating oil at room temperature or under heating, and further drying.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27922086A JPS63132947A (en) | 1986-11-21 | 1986-11-21 | Method for treating molded polyamide article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27922086A JPS63132947A (en) | 1986-11-21 | 1986-11-21 | Method for treating molded polyamide article |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63132947A true JPS63132947A (en) | 1988-06-04 |
JPH0555535B2 JPH0555535B2 (en) | 1993-08-17 |
Family
ID=17608100
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27922086A Granted JPS63132947A (en) | 1986-11-21 | 1986-11-21 | Method for treating molded polyamide article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63132947A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107868267A (en) * | 2017-12-15 | 2018-04-03 | 丹阳市金晟医用橡塑制品有限公司 | A kind of method for lifting medical natural rubber injection member and piston ageing resistace |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6038439A (en) * | 1983-08-12 | 1985-02-28 | Ube Ind Ltd | Treatment of polyamide molding |
-
1986
- 1986-11-21 JP JP27922086A patent/JPS63132947A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6038439A (en) * | 1983-08-12 | 1985-02-28 | Ube Ind Ltd | Treatment of polyamide molding |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107868267A (en) * | 2017-12-15 | 2018-04-03 | 丹阳市金晟医用橡塑制品有限公司 | A kind of method for lifting medical natural rubber injection member and piston ageing resistace |
Also Published As
Publication number | Publication date |
---|---|
JPH0555535B2 (en) | 1993-08-17 |
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